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(Received for publication, October 19, 1995, and in revised form, March 15, 1996)
From the Departments of Medicine and Pathology, Washington
University School of Medicine, St. Louis, Missouri 63110
Members of the Janus kinase (Jak) family of
protein tyrosine kinases have recently been implicated in the proximal
signal transduction events of cytokine receptors. Jak3, a newly
discovered member of this family, is believed to be normally limited in
its expression to cells of the lymphoid and myeloid lineages. Herein we
show that Jak3 is expressed in primary human vascular cells, as well as
other non-lymphoid and non-myeloid cell types. Reverse
transcriptase-polymerase chain reaction and Northern blot analysis
revealed that Jak3 mRNA was expressed at low levels in human
umbilical vein endothelial cells (HUVEC), human aortic smooth muscle
cells (HASMC), A549 (human lung carcinoma), and DLD-1 (human colon
adenocarcinoma) cells. Higher basal levels of Jak3 mRNA were
detected in HMEC-1 (human microvascular cell line) and HepG2 (human
hepatocellular carcinoma) cells. Jak3 mRNA expression was induced
in HUVEC, HMEC-1, and HASMC by treatment with interleukin-1
Volume 271, Number 24,
Issue of June 14, 1996
pp. 13976-13980
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
, tumor
necrosis factor-
, interferon-
, and lipopolysaccharide. Jak3
protein was detectable at low levels in untreated HMEC-1, and these
levels increased significantly with cytokine treatment. Furthermore,
Jak3 protein was phosphorylated upon treatment of these cells with
interleukin-4. This work shows that Jak3 is expressed or inducible in
human vascular endothelial, vascular smooth muscle, and other
non-lymphoid and non-myeloid cells, suggesting a broader role for Jak3
in the cytokine signal transduction of these cells.
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